Litcius/Paper detail

Stabilization of an Enantiopure Sub‐monolayer of Helicene Radical Cations on a Au(111) Surface through Noncovalent Interactions

Niccolò Giaconi, Andrea Luigi Sorrentino, Lorenzo Poggini, Michela Lupi, Vincent Polewczyk, Giovanni Vinai, Piero Torelli, Agnese Magnani, Roberta Sessoli, Stefano Menichetti, Lorenzo Sorace, Caterina Viglianisi, Matteo Mannini

2021Angewandte Chemie International Edition19 citationsDOIOpen Access PDF

Abstract

In the past few years, the chirality and magnetism of molecules have received notable interest for the development of novel molecular devices. Chiral helicenes combine both these properties, and thus their nanostructuration is the first step toward developing new multifunctional devices. Here, we present a novel strategy to deposit a sub-monolayer of enantiopure thia[4]helicene radical cations on a pre-functionalized Au(111) substrate. This approach results in both the paramagnetic character and the chemical structure of these molecules being maintained at the nanoscale, as demonstrated by in-house characterizations. Furthermore, synchrotron-based X-ray natural circular dichroism confirmed that the handedness of the thia[4]helicene is preserved on the surface.

Topics & Concepts

Enantiopure drugHeliceneChirality (physics)MonolayerMoleculeMagnetismCircular dichroismChemistrySubstrate (aquarium)CrystallographyMaterials scienceNanotechnologyEnantioselective synthesisOrganic chemistryCatalysisCondensed matter physicsPhysicsOceanographyChiral symmetry breakingNambu–Jona-Lasinio modelGeologyQuarkQuantum mechanicsSynthesis and Properties of Aromatic CompoundsGraphene research and applicationsSurface Chemistry and Catalysis